Introduction The less we know about something, the greater the need to constantly redefine it. (P. G. McDonough [1]) Polycystic ovary syndrome (PCOS) affects 6-10% of reproductive age females, making it the most common metabolic endocrine condition in this population [2]. PCOS was first officially described in 1935 by Drs. Stein and Leventhal, resulting in its eponymous name, the Stein-Leventhal syndrome. The syndrome they described were patients who presented with amenorrhea, hirsutism, polycystic-appearing ovaries, and oft en obesity. They described the operation known as a "wedge resection," which was oft en followed by regular menses and sometimes pregnancy. On pathological examination of tissue from the ovarian "wedge resection," they noted multiple subcapsular cysts associated with a thickening of the tunica [3]. Later, this constellation of signs and symptoms became known as PCOS, which reflected the multiple subcapsular follicular cysts. Since 1935, our understanding of this syndrome has expanded and in 2012 an evidence-based methodology workshop was sponsored by the National Institutes of Health. At this workshop one recommendation was to change the name from PCOS to more closely reflect the complex pathophysiology of this condition, which would improve accurate communication and progress in both the clinical and research arenas [4]. Nature vs. nurture PCOS is a complex condition characterized by anovulation and androgen overproduction affecting reproductive age women. Th is phenotype can result in infertility due to ovulatory dysfunction, irregular menses, endometrial hyperplasia, endometrial carcinoma, iron deficiency anemia due to heavy menses, hirsutism, virilization, miscarriage, insulin resistance, glucose intolerance, gestational and type 2 diabetes mellitus, hyperlipidemia, and the potential for increased risk of cardiovascular disease. Other conditions associated with PCOS include obesity, sleep apnea, anxiety, depression, and possible reduction in quality of life. Studies have demonstrated a strong genetic component, supported by family and twin studies, with an important environmental contribution.